Compound ID | 3291
Synonym(s): MK7762 | MK 7762 | TBD 09 | TBD-09
Class: Oxazolidinone
Details of activity: | Active against Mycobacterium tuberculosis; protein synthesis inhibitor (targets 50S ribosomal subunit) |
Description: | Synthetic compound |
Institute where first reported: | Bill & Melinda Gates Medical Research Institute; Merck |
Year first mentioned: | 2023 |
Highest developmental phase: | Phase 1 (NCT05824091) |
Development status: | Active (as of 2024) |
Chemical structure(s): | |
Canonical SMILES: | COC(=O)NC[C@H]1CN(C2=CC(=C(C(=C2)F)N3CCS(=O)(=O)CC3)F)C(=O)O1 |
Isomeric SMILES: | COC(=O)NC[C@H]1CN(C(=O)O1)C2=CC(=C(C(=C2)F)N3CCS(=O)(=O)CC3)F |
InChI: | InChI=1S/C16H19F2N3O6S/c1-26-15(22)19-8-11-9-21(16(23)27-11)10-6-12(17)14(13(18)7-10)20-2-4-28(24,25)5-3-20/h6-7,11H,2-5,8-9H2,1H3,(H,19,22)/t11-/m0/s1 |
InChI Key: | CCYKSCLMFZLAJH-NSHDSACASA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/156857753 |
External links: | |
Main Source: | https://www.newtbdrugs.org/pipeline/compound/tbd09-mk7762 |